Canonical Allele Identifier: CA1107106
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095451
ClinVar RCV Id: RCV004386769
dbSNP Id: rs373305550
ExAC: 1:152284801 C / T
gnomAD v2: 1-152284801-C-T
gnomAD v3: 1-152312325-C-T
gnomAD v4: 1-152312325-C-T
MyVariant Identifiers: chr1:g.152284801C>T (hg19) chr1:g.152312325C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312325C>T , CM000663.2:g.152312325C>T GRCh38
NC_000001.10:g.152284801C>T , CM000663.1:g.152284801C>T GRCh37
NC_000001.9:g.150551425C>T NCBI36
NG_016190.1:g.17879G>A , LRG_1028:g.17879G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2561G>A MANE Select ENSP00000357789.1:p.Gly854Glu
ENST00000368799.1:c.2561G>A ENSP00000357789.1:p.Gly854Glu
NM_002016.1:c.2561G>A , LRG_1028t1:c.2561G>A NP_002007.1:p.Gly854Glu
XM_011509329.1:c.2561G>A XP_011507631.1:p.Gly854Glu
NM_002016.2:c.2561G>A MANE Select NP_002007.1:p.Gly854Glu
Search 100 bp 5'
Search 100 bp 3'